Sophoraflavonoloside

Base Information

• Chemical Name: Sophoraflavonoloside
• CAS No.: 19895-95-5
• Deprecated CAS: 103615-79-8,76501-44-5,27214-53-5,69493-38-5
• Molecular Formula: C₂₇H₃₀O₁₆
• Molecular Weight: 610.526
• UNII: 3C1196Z645
• ChEMBL ID: CHEMBL2032411
• DSSTox Substance ID: DTXSID20941769
• Metabolomics Workbench ID: 70536
• Nikkaji Number: J94.447E
• Wikidata: Q27114674
• Mol file: 19895-95-5.mol

Synonyms:kaempferol 3-O-sophoroside

Chemical Property of Sophoraflavonoloside

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 194-198℃
• Boiling Point: 995°Cat760mmHg
• PKA: 6.20±0.40(Predicted)
• Flash Point: 329.2°C
• PSA: 269.43000
• Density: 1.82g/cm³
• LogP: -2.42030
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility.: DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly), Water (Slightly)
• XLogP3: -0.9
• Hydrogen Bond Donor Count: 10
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 7
• Exact Mass: 610.15338487
• Heavy Atom Count: 43
• Complexity: 1000

Purity/Quality:

≥98% ^*data from raw suppliers

Kaempferol3-β-Sophoroside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O
• Isomeric SMILES: C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O
• Uses: Kaempferol 3-β-Sophoroside is a derivative of Kaempferol (K100000), a plant flavonoid which play a beneficial role in human health promotion.

Technology Process of Sophoraflavonoloside

There total 5 articles about Sophoraflavonoloside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 50.0%

kaempferol-3-sophoroside-7-α-L-arabinofuranoside (132998-80-2) → kaempferol-3-O-sophoroside (19895-95-5,31512-06-8)

Guidance literature:

With sodium hydroxide; for 3h; Ambient temperature;

DOI:10.1016/0031-9422(90)85359-N

Reference yield:

kaempferol 3-O-β-D-[β-D-glucopyranosyl-(1→2)-glucopyranoside]-7-O-β-D-glucopyranoside (55136-76-0) → kaempferol-3-O-sophoroside (19895-95-5,31512-06-8)

Guidance literature:

β-glucosidase; at 37 ℃; for 5h;

DOI:10.1248/cpb.35.97

Reference yield:

3-O-β-sophorosyl-7-O-β-D-(2-O-feruloyl)glucosylkaempferol (87863-90-9) → kaempferol-3-O-sophoroside (19895-95-5,31512-06-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 13 mg / 1 percent KOH

2: 12 mg / β-glucosidase / 5 h / 37 °C

With potassium hydroxide; β-glucosidase;

DOI:10.1248/cpb.35.97

upstream raw materials:

kaempferol 3-O-β-D-[β-D-glucopyranosyl-(1→2)-glucopyranoside]-7-O-β-D-glucopyranoside

kaempferol-3-sophoroside-7-α-L-arabinofuranoside

3-O-β-sophorosyl-7-O-β-D-(2-O-feruloyl)glucosylkaempferol

Downstream raw materials:

kaempferol

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